Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
2548 | 2211 | 40.0 | 83% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
0 | 4 | BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY | 4064930 |
196 | 3 | GENETICS & HEREDITY//FRAGILE X SYNDROME//AMERICAN JOURNAL OF MEDICAL GENETICS | 53756 |
1566 | 2 | FRAGILE X SYNDROME//RETT SYNDROME//FRAGILE X | 7353 |
2548 | 1 | RETT SYNDROME//MECP2//CDKL5 | 2211 |
Terms with highest relevance score |
rank | Term | termType | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|---|
1 | RETT SYNDROME | authKW | 9399828 | 38% | 82% | 830 |
2 | MECP2 | authKW | 3323133 | 16% | 69% | 350 |
3 | CDKL5 | authKW | 639138 | 2% | 86% | 54 |
4 | MECP2 GENE | authKW | 538546 | 2% | 100% | 39 |
5 | MECP2 MUTATION | authKW | 372839 | 1% | 100% | 27 |
6 | METHYL CPG BINDING PROTEIN 2 | authKW | 362172 | 2% | 66% | 40 |
7 | WESTERN SYDNEY GENET PROGRAM | address | 340342 | 3% | 39% | 63 |
8 | BRAIN & DEVELOPMENT | journal | 210339 | 11% | 6% | 235 |
9 | RETT | address | 194185 | 1% | 94% | 15 |
10 | PRESERVED SPEECH VARIANT | authKW | 179515 | 1% | 100% | 13 |
Web of Science journal categories |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | Clinical Neurology | 11891 | 32% | 0% | 717 |
2 | Genetics & Heredity | 6936 | 24% | 0% | 531 |
3 | Pediatrics | 5866 | 18% | 0% | 406 |
4 | Neurosciences | 2452 | 21% | 0% | 468 |
5 | Education, Special | 1106 | 2% | 0% | 52 |
6 | Rehabilitation | 918 | 5% | 0% | 102 |
7 | Psychology, Developmental | 633 | 3% | 0% | 72 |
8 | Biochemistry & Molecular Biology | 322 | 14% | 0% | 320 |
9 | Psychiatry | 306 | 5% | 0% | 118 |
10 | Cell Biology | 112 | 6% | 0% | 128 |
Address terms |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | WESTERN SYDNEY GENET PROGRAM | 340342 | 3% | 39% | 63 |
2 | RETT SYNDROME | 196389 | 1% | 89% | 16 |
3 | RETT | 194185 | 1% | 94% | 15 |
4 | GENET EPIGENET CONTROL GENE EXP S | 139238 | 0% | 92% | 11 |
5 | TUSCANY RETT | 96662 | 0% | 100% | 7 |
6 | CIVITAN INT | 87778 | 2% | 17% | 38 |
7 | BLUE BIRD CIRCLE RETT | 82853 | 0% | 100% | 6 |
8 | P PATHOPHYSIOL REHABIL UNIT | 75178 | 0% | 78% | 7 |
9 | SAN RAFFAELE RETT | 75178 | 0% | 78% | 7 |
10 | SAN RAFFAELE RETT UNIT | 75178 | 0% | 78% | 7 |
Journals |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | BRAIN & DEVELOPMENT | 210339 | 11% | 6% | 235 |
2 | JOURNAL OF CHILD NEUROLOGY | 30720 | 5% | 2% | 104 |
3 | NEUROPEDIATRICS | 13109 | 2% | 2% | 44 |
4 | PEDIATRIC NEUROLOGY | 8088 | 2% | 1% | 50 |
5 | EUROPEAN CHILD & ADOLESCENT PSYCHIATRY | 7139 | 1% | 2% | 28 |
6 | AMERICAN JOURNAL OF MEDICAL GENETICS | 6989 | 3% | 1% | 67 |
7 | EUROPEAN JOURNAL OF HUMAN GENETICS | 6609 | 2% | 1% | 42 |
8 | JOURNAL OF NEURODEVELOPMENTAL DISORDERS | 6356 | 0% | 4% | 11 |
9 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 5443 | 2% | 1% | 48 |
10 | HUMAN MOLECULAR GENETICS | 5180 | 3% | 1% | 61 |
Author Key Words |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | RETT SYNDROME | 9399828 | 38% | 82% | 830 | Search RETT+SYNDROME | Search RETT+SYNDROME |
2 | MECP2 | 3323133 | 16% | 69% | 350 | Search MECP2 | Search MECP2 |
3 | CDKL5 | 639138 | 2% | 86% | 54 | Search CDKL5 | Search CDKL5 |
4 | MECP2 GENE | 538546 | 2% | 100% | 39 | Search MECP2+GENE | Search MECP2+GENE |
5 | MECP2 MUTATION | 372839 | 1% | 100% | 27 | Search MECP2+MUTATION | Search MECP2+MUTATION |
6 | METHYL CPG BINDING PROTEIN 2 | 362172 | 2% | 66% | 40 | Search METHYL+CPG+BINDING+PROTEIN+2 | Search METHYL+CPG+BINDING+PROTEIN+2 |
7 | RETT | 184618 | 1% | 70% | 19 | Search RETT | Search RETT |
8 | PRESERVED SPEECH VARIANT | 179515 | 1% | 100% | 13 | Search PRESERVED+SPEECH+VARIANT | Search PRESERVED+SPEECH+VARIANT |
9 | FOXG1 | 176901 | 1% | 41% | 31 | Search FOXG1 | Search FOXG1 |
10 | METHYL CPG BINDING PROTEIN 2 MECP2 | 150357 | 1% | 78% | 14 | Search METHYL+CPG+BINDING+PROTEIN+2+MECP2 | Search METHYL+CPG+BINDING+PROTEIN+2+MECP2 |
Core articles |
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c: (1) Number of references referring to publications in the class. (2) Share of total number of active references referring to publications in the class. (3) Age of the article. New articles get higher score than old articles. (4) Citation rate, normalized to year. |
Rank | Reference | # ref. in cl. |
Shr. of ref. in cl. |
Citations |
---|---|---|---|---|
1 | LIYANAGE, VRB , RASTEGAR, M , (2014) RETT SYNDROME AND MECP2.NEUROMOLECULAR MEDICINE. VOL. 16. ISSUE 2. P. 231-264 | 216 | 80% | 14 |
2 | LEONARD, H , COBB, S , DOWNS, J , (2017) CLINICAL AND BIOLOGICAL PROGRESS OVER 50 YEARS IN RETT SYNDROME.NATURE REVIEWS NEUROLOGY. VOL. 13. ISSUE 1. P. 37 -51 | 193 | 95% | 0 |
3 | CHAHROUR, M , ZOGHBI, HY , (2007) THE STORY OF RETT SYNDROME: FROM CLINIC TO NEUROBIOLOGY.NEURON. VOL. 56. ISSUE 3. P. 422-437 | 112 | 93% | 531 |
4 | LOMBARDI, LM , BAKER, SA , ZOGHBI, HY , (2015) MECP2 DISORDERS: FROM THE CLINIC TO MICE AND BACK.JOURNAL OF CLINICAL INVESTIGATION. VOL. 125. ISSUE 8. P. 2914 -2923 | 114 | 84% | 24 |
5 | LYST, MJ , BIRD, A , (2015) RETT SYNDROME: A COMPLEX DISORDER WITH SIMPLE ROOTS.NATURE REVIEWS GENETICS. VOL. 16. ISSUE 5. P. 261 -274 | 109 | 78% | 29 |
6 | GUY, J , CHEVAL, H , SELFRIDGE, J , BIRD, A , (2011) THE ROLE OF MECP2 IN THE BRAIN.ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 27. VOL. 27. ISSUE . P. 631-652 | 104 | 82% | 176 |
7 | KATZ, DM , BERGER-SWEENEY, JE , EUBANKS, JH , JUSTICE, MJ , NEUL, JL , POZZO-MILLER, L , BLUE, ME , CHRISTIAN, D , CRAWLEY, JN , GIUSTETTO, M , ET AL (2012) PRECLINICAL RESEARCH IN RETT SYNDROME: SETTING THE FOUNDATION FOR TRANSLATIONAL SUCCESS.DISEASE MODELS & MECHANISMS. VOL. 5. ISSUE 6. P. 733-745 | 112 | 85% | 43 |
8 | CALFA, G , PERCY, AK , POZZO-MILLER, L , (2011) EXPERIMENTAL MODELS OF RETT SYNDROME BASED ON MECP2 DYSFUNCTION.EXPERIMENTAL BIOLOGY AND MEDICINE. VOL. 236. ISSUE 1. P. 3 -19 | 121 | 74% | 49 |
9 | KATZ, DM , BIRD, A , COENRAADS, M , GRAY, SJ , MENON, DU , PHILPOT, BD , TARQUINIO, DC , (2016) RETT SYNDROME: CROSSING THE THRESHOLD TO CLINICAL TRANSLATION.TRENDS IN NEUROSCIENCES. VOL. 39. ISSUE 2. P. 100 -113 | 80 | 74% | 8 |
10 | DELLA SALA, G , PIZZORUSSO, T , (2014) SYNAPTIC PLASTICITY AND SIGNALING IN RETT SYNDROME.DEVELOPMENTAL NEUROBIOLOGY. VOL. 74. ISSUE 2. P. 178-196 | 115 | 71% | 12 |
Classes with closest relation at Level 1 |